Belmont Medical 3-Spike Disposable Set (part 903-00006) used with RI-2 infusers may leak during priming due to a female quick connector crack, risking treatment delays. Affected units have specific lot numbers.
Disposable set may leak during priming from a female quick connector due to a crack in the female quick connector, may lead to a potential delay in treatment since the set will need to be replaced by another set
Belmont Medical 3-Spike Disposable Sets used with the RI-2 infuser may leak during priming because of a crack in the quick connector, which could delay treatment. This recall affects hospital and care environments where warmed blood or fluids are administered to patients.
The disposable set has a crack in the female quick connector that may leak during priming. This leak could require replacing the set, causing delays in treatment for patients needing warmed blood or fluids.
Healthcare workers using the Belmont Medical 3-Spike Disposable Set with the RI-2 infuser in hospitals or care facilities are most at risk. Patients receiving warmed blood or fluids through this system could experience treatment delays.
Check for part number 903-00006 on the set. Affected units were sold with lot numbers 20240910, 20241002, 20241006, or 20241014.
Inspect the female quick connector for cracks before use to ensure no leaks occur during priming.
The set may leak during priming due to a crack in the female quick connector, which could require replacing the set and delay treatment.
The part number is 903-00006 for the Belmont Medical 3-Spike Disposable Set.
Lot numbers 20240910, 20241002, 20241006, and 20241014 are affected.
We’ve drafted a message you can send Belmont to request your refund or repair — edit it as you like.
Subject: Recall Z-1099-2025 — Belmont Belmont Hello, I own a Belmont that is covered by recall Z-1099-2025 from Belmont. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
